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单域抗体-金纳米粒子生物缀合物作为汉坦病毒检测的免疫传感器。

Single-Domain Antibody-Gold Nanoparticle Bioconjugates as Immunosensors for the Detection of Hantaviruses.

机构信息

Fundação Oswaldo Cruz, FIOCRUZ, Fiocruz Rondônia, Porto Velho, RO, Brazil.

Programa de Pós-graduação em Biologia Experimental, PGBIOEXP, Universidade Federal de Rondônia, UNIR, Porto Velho, RO, Brazil.

出版信息

Mol Diagn Ther. 2024 Jul;28(4):479-494. doi: 10.1007/s40291-024-00713-1. Epub 2024 May 26.

Abstract

INTRODUCTION

Hantavirus, a zoonotic pathogen, causes severe syndromes like hemorrhagic fever with renal syndrome (HFRS), sometimes fatal in humans. Considering the importance of detecting the hantavirus antigen, the construction of an immunosensor is essential. The structural and functional characteristics of camelid nanobodies (VHHs) encourage their application in the areas of nanobiotechnology, therapeutics, diagnostics, and basic research. Therefore, this study aimed to standardize stable bioconjugates using gold nanoparticles (AuNPs) and VHHs, in order to develop immunobiosensors for the diagnosis of hantavirus infection.

METHODS

Immobilized metal affinity chromatography (IMAC) was performed to obtain purified recombinant anti-hantavirus nucleocapsid nanobodies (anti-prNΔ VHH), while AuNPs were synthesized for bioconjugation. UV-visible spectrophotometry and transmission electron microscopy (TEM) analysis were employed to characterize AuNPs.

RESULTS

The bioconjugation stability parameters (VHH-AuNPs), analyzed by spectrophotometry, showed that the ideal pH value and VHH concentration were obtained at 7.4 and 50 μg/mL, respectively, after addition of 1 M NaCl, which induces AuNP aggregation. TEM performed before and after bioconjugation showed uniform, homogeneous, well-dispersed, and spherical AuNPs with an average diameter of ~ 14 ± 0.57 nm. Furthermore, high-resolution images revealed a thin white halo on the surface of the AuNPs, indicating the coating of the AuNPs with protein. A biosensor simulation test (dot blot-like [DB-like]) was performed in stationary phase to verify the binding and detection limits of the recombinant nucleocapsid protein from the Araucária hantavirus strain (prN∆).

DISCUSSION

Using AuNPs/VHH bioconjugates, a specific interaction was detected between 5 and 10 min of reaction in a dose-dependent manner. It was observed that this test was sensitive enough to detect prNΔ at concentrations up to 25 ng/μL. Considering that nanostructured biological systems such as antibodies conjugated with AuNPs are useful tools for the development of chemical and biological sensors, the stability of the bioconjugate indicates proficiency in detecting antigens. The experimental results obtained will be used in a future immunospot assay or lateral flow immunochromatography analysis for hantavirus detection.

摘要

简介

汉坦病毒是一种人畜共患病病原体,可导致人类出现严重综合征,如肾综合征出血热(HFRS),有时甚至致命。鉴于检测汉坦病毒抗原的重要性,免疫传感器的构建至关重要。骆驼科纳米抗体(VHH)的结构和功能特性鼓励将其应用于纳米生物技术、治疗学、诊断学和基础研究领域。因此,本研究旨在使用金纳米颗粒(AuNPs)和 VHH 来标准化稳定的生物缀合物,以便开发用于诊断汉坦病毒感染的免疫生物传感器。

方法

采用固定化金属亲和层析(IMAC)法获得纯化的重组抗汉坦病毒核衣壳纳米抗体(抗-prNΔ VHH),同时合成 AuNPs 进行生物缀合。采用紫外-可见分光光度法和透射电子显微镜(TEM)分析对 AuNPs 进行了表征。

结果

通过分光光度法分析的生物缀合稳定性参数(VHH-AuNPs)表明,在添加 1 M NaCl 诱导 AuNP 聚集后,最佳 pH 值和 VHH 浓度分别为 7.4 和 50 μg/mL。TEM 分析显示,生物缀合前后 AuNPs 均匀、均匀、分散良好且呈球形,平均直径约为 14 ± 0.57nm。此外,高分辨率图像显示 AuNPs 表面有一层薄的白色晕圈,表明 AuNPs 表面涂覆了蛋白质。在固定相上进行生物传感器模拟试验(点印迹样[DB-样]),以验证 Araucária 汉坦病毒株(prN∆)的重组核衣壳蛋白的结合和检测限。

讨论

采用 AuNPs/VHH 生物缀合物,以剂量依赖的方式在 5-10 分钟的反应时间内检测到特异性相互作用。结果表明,该试验的灵敏度足以检测到浓度高达 25ng/μL 的 prNΔ。考虑到纳米结构的生物系统,如与 AuNPs 缀合的抗体,是开发化学和生物传感器的有用工具,生物缀合物的稳定性表明其能够有效地检测抗原。实验结果将用于未来的免疫斑点分析或汉坦病毒检测的侧向流动免疫层析分析。

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